Computer Training and Transcranial Direct Current Stimulation for Cognition in HIV

Sponsor
Nova Southeastern University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03440840
Collaborator
(none)
42
1
3
57.5
0.7

Study Details

Study Description

Brief Summary

This study investigates the effectiveness of computer-based cognitive training with or without transcranial direct current stimulation (tDCS) in improving the functioning of older individuals with HIV-related cognitive dysfunction.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Transcranial Direct Current Stimulation (tDCS)
  • Behavioral: Computer-based Cognitive Training
  • Behavioral: Watching Educational Videos
N/A

Detailed Description

In spite of advances in its treatment, persons with HIV continue to develop HIV-associated neurocognitive disorders (HAND) over time. HAND may be an even more significant problem in older persons (age 50+) with HIV who may experience age-related changes in cognition in addition to HAND. Because of HAND's impact on patients' functioning and quality of life, treatments are needed. Pharmacologic treatments have, in general, been ineffective and investigators have argued that computer delivered cognitive training may be an effective alternative. While results of small studies have been encouraging, the effect size of cognitive training may be small and of unclear practical importance. The nature of cognitive training programs, often building on laboratory measures of cognition, may reduce how inherently interesting (i.e., fun) they are, limiting their uptake outside of paid research studies. Others have argued for the use of computer games targeting psychomotor speed, problem solving, and visuospatial skills to improve cognitive function in older adults. Data support the utility of this approach, but again effect sizes may be small.

Transcranial direct current stimulation (tDCS) may be an effective way to enhance the effects of cognitive training. It involves the application of a small electric current (1-2 mA) to the head, inducing small currents within the brain that enhance cognitive training. Multiple studies have shown that tDCS enhances cognition, including attention and psychomotor speed. The investigators previously completed a single-blind pilot study of individuals with HIV-related mild neurocognitive disorder using a high-interest car racing game with or without tDCS. Results were encouraging in showing moderate to large effect sizes consistent with tDCS enhancement of cognitive function after six 20-minute training sessions over two weeks. Participants' subjective reports of cognitive difficulties supported observed effects on objective measures, and their mood improved. The intervention was acceptable to participants, many of whom stated they enjoyed it. Everyone indicated a willingness to participate in a similar study in the future.

In this study the investigators will expand on a pilot-tested training intervention with 120 individuals randomly assigned to an attention control condition or game-based cognitive training with either sham or active tDCS. The investigators will employ a battery of cognitive measures as well as self-report measures of mood, cognitive difficulties, and everyday functioning in order to evaluate the effects of study interventions.

Participants will first be screened for eligibility by telephone, and then scheduled for a visit during which their eligibility will be further assessed. Those who are eligible based on inclusion and exclusion criteria will complete a battery of measures of their cognitive and functional status. They will then complete six training sessions over a period of three weeks, and then once again complete the battery of assessments. Participants will then be asked to return one month after the post-training assessment to evaluate the persistence of training effects.

Study Design

Study Type:
Interventional
Actual Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized parallel groupRandomized parallel group
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Individuals will receive either active or sham tDCS. The outcomes assessor will be blind to treatment group assignment.
Primary Purpose:
Treatment
Official Title:
Computer Training and Transcranial Direct Current Stimulation for Cognition in HIV
Actual Study Start Date :
Jan 16, 2018
Actual Primary Completion Date :
Oct 15, 2019
Anticipated Study Completion Date :
Nov 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Computer Training with active tDCS

Participants randomized to this arm will receive computer-based cognitive training using a car racing game with active transcranial direct current stimulation (tDCS).

Procedure: Transcranial Direct Current Stimulation (tDCS)
Application of a small electrical current (1-2 mA) across the head.
Other Names:
  • tDCS
  • Behavioral: Computer-based Cognitive Training
    Use of computer-delivered games or exercises with the goal of improving cognitive performance.
    Other Names:
  • Cognitive Training
  • Active Comparator: Computer Training with sham tDCS

    Participants randomized to this arm will receive computer-based cognitive training using a car racing game with sham transcranial direct current stimulation (tDCS).

    Behavioral: Computer-based Cognitive Training
    Use of computer-delivered games or exercises with the goal of improving cognitive performance.
    Other Names:
  • Cognitive Training
  • Placebo Comparator: Computer Training with or without tDCS

    Participants in this arm will watch educational videos as a comparator to computer training with the car racing game (watching educational videos).

    Procedure: Transcranial Direct Current Stimulation (tDCS)
    Application of a small electrical current (1-2 mA) across the head.
    Other Names:
  • tDCS
  • Behavioral: Watching Educational Videos
    Watching educational videos and answering questions about them

    Outcome Measures

    Primary Outcome Measures

    1. Psychomotor speed [3 weeks]

      Ability of the participant to attend to and use complex stimuli while making a motor response

    Secondary Outcome Measures

    1. Functional Status [3 weeks]

      Participant performance on observed tasks of daily living

    2. Participant Assessment of Own Functioning (PAOF) [3 weeks]

      Participant self-report of issues related to cognitive and sensory functioning

    3. Center for Epidemiological Studies Depression scale (CES-D) [3 weeks]

      Participant self-report of mood

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Treated with antiretroviral medication for at least one month

    • Meet criteria for Mild Neurocognitive Disorder

    Exclusion Criteria:
    • Seizure disorder

    • Recent head injury or surgery

    • Personal or family history of bipolar disorder;

    • Some medications

    • Left handedness

    • HIV Dementia

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 NSU Psychiatry Research Office Fort Lauderdale Florida United States 33328

    Sponsors and Collaborators

    • Nova Southeastern University

    Investigators

    • Principal Investigator: Raymond L Ownby, MD, PhD, Nova Southeastern University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Raymond Ownby, M.D., Professor and Chair, Nova Southeastern University
    ClinicalTrials.gov Identifier:
    NCT03440840
    Other Study ID Numbers:
    • AG056256
    First Posted:
    Feb 22, 2018
    Last Update Posted:
    Jul 2, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 2, 2021